مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Verion

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

video

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

sound

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Version

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View:

1,151
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

0
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

EVALUATION AND COMPARISON OF ENZYME IMMUNOASSAY (EIA) AND ACID FAST STAINING WITH CONFIRMATION BY IMMUNOFLUORESCENT ANTIBODY ASSAY FOR DETECTION OF CRYPTOSPORIDIUM SPECIES IN INFANTS AND YOUNG CHILDREN.

Pages

  10-10

Keywords

ENZYME IMMUNOASSAY (EIA)Q4
IMMUNOFLUORESCENT ANTIBODY ASSAY (IFA)Q4

Abstract

 Introduction: Cryptosporidiosis is prevalent world wide, causing a variety of problems ranging from acute, self-limiting diarrhea to fatal cases in immunocompromised persons, particulary those with acquired immunodeficiency (AIDS). Diagnosis of CRYPTOSPORIDIUM is made by identification of oocysts in stool specimens. The detection is most commonly made by the acid-fast staining method followed by microscopic examination which has low specificity and sensitivity. Material and Methods: In the present study, we evaluated diagnostic utility of a commercially available enzyme immunoassay (EIA), which detects CRYPTOSPORIDIUM-Specific antigen (CSA) in 204 unprocessed stool specimens obtained from patients less than 3 years of age. Results: When compared with the routine screening procedure applied in this field study (screening by acidfast staining and microscopy after concentration of positive results by IFA), both sensitivity and specificity were 98%. Of the 139 specimens negative by microscopy, 13 (9.3%) were positive by EIA, 11 of which were confirmed by inhibition with antibody to Cryptosporidia-specific antigen. Conclusion: The EIA is an important tool for identifying CRYPTOSPORIDIUM in fecal specimens in field studies since it is sensitive, specific, simple to use and unaffected by the presence of a preservative.

Cites

  • No record.
  • References

  • No record.
  • Cite

    APA: Copy

    DOROSTCAR MOGHADDAM, D., & AZAMI, M.. (2005). EVALUATION AND COMPARISON OF ENZYME IMMUNOASSAY (EIA) AND ACID FAST STAINING WITH CONFIRMATION BY IMMUNOFLUORESCENT ANTIBODY ASSAY FOR DETECTION OF CRYPTOSPORIDIUM SPECIES IN INFANTS AND YOUNG CHILDREN.. JOURNAL OF SHAHID SADOUGHI UNIVERSITY OF MEDICAL SCIENCES, 12(4), 10-10. SID. https://sid.ir/paper/378202/en

    Vancouver: Copy

    DOROSTCAR MOGHADDAM D., AZAMI M.. EVALUATION AND COMPARISON OF ENZYME IMMUNOASSAY (EIA) AND ACID FAST STAINING WITH CONFIRMATION BY IMMUNOFLUORESCENT ANTIBODY ASSAY FOR DETECTION OF CRYPTOSPORIDIUM SPECIES IN INFANTS AND YOUNG CHILDREN.. JOURNAL OF SHAHID SADOUGHI UNIVERSITY OF MEDICAL SCIENCES[Internet]. 2005;12(4):10-10. Available from: https://sid.ir/paper/378202/en

    IEEE: Copy

    D. DOROSTCAR MOGHADDAM, and M. AZAMI, “EVALUATION AND COMPARISON OF ENZYME IMMUNOASSAY (EIA) AND ACID FAST STAINING WITH CONFIRMATION BY IMMUNOFLUORESCENT ANTIBODY ASSAY FOR DETECTION OF CRYPTOSPORIDIUM SPECIES IN INFANTS AND YOUNG CHILDREN.,” JOURNAL OF SHAHID SADOUGHI UNIVERSITY OF MEDICAL SCIENCES, vol. 12, no. 4, pp. 10–10, 2005, [Online]. Available: https://sid.ir/paper/378202/en

    Related Journal Papers

    Related Seminar Papers

  • No record.
  • Related Plans

  • No record.
  • Recommended Workshops






    Move to top
    telegram sharing button
    whatsapp sharing button
    linkedin sharing button
    twitter sharing button
    email sharing button
    email sharing button
    email sharing button
    sharethis sharing button